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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539506Generated: October 26, 2026

Carbamate → (Quinolin-3-yl)methanol

https://huagongshe.com/reaction/539506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbamateHCID 276—
ReactantQuinolineHCID 7047—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product(Quinolin-3-yl)methanolHCID 12662983—

Reaction Steps

Synthesis of compounds ERW1041A, B, C, D, E, and 1069 were synthesized using the methods of Choi et al. Chemistry & Biology, Volume 12, Issue 4, Pages 469-475, except the amino-acid amines are protected by a quinoline-containing carbamate. This quinoline-containing carbamate is synthesized by reducing 3-quinolylcarbaldehyde with sodium borohydride in THF followed by an aqueous workup and flash chromatography yielding 3-quinolylcarbinol. para-Nitro-phenylchloroformate is reacted with 3-quinolylcarbinol in methylene chloride and N-methyl morpholine to give a carbonate of 3-quinoline methanol and para-Nitro-phenol. After purification by flash chromatography, this carbonate is reacted with the methyl ester of the amino acid in neat DMF to give the named compounds.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871718B2
Source datasetuspto-grants-2014_10
ORD IDord-081ecec58c714981b4aae8a58db36932
Source noteuspto-grants-2014_10